Evidence map›Paper›PMID 25417649›Full record

ArticleNature communications2014

Retinoid X receptor α attenuates host antiviral response by suppressing type I interferon.

Feng Ma, Su-Yang Liu, Bahram Razani, Neda Arora, Bing Li, Hiroyuki Kagechika, Peter Tontonoz, Vanessa Núñez, Mercedes Ricote, Genhong Cheng

Open access · bronzeAbstract read
In one paragraph

Article in Nature communications, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
1.1field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
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  4. Genetic ancestry shapes dengue virus infection in human skin explants.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  6. UTX (KDM6A) promotes differentiation noncatalytically in somatic self-renewing epithelia.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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  16. Amplified Gliosis and Interferon-Associated Inflammation in the Aging Brain following Diffuse Traumatic Brain Injury.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  17. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 3 countries.

Feng MaDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, California 90095, USA.
Su-Yang LiuDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, California 90095, USA.
Bahram RazaniDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, California 90095, USA.
Neda AroraDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, California 90095, USA.
Bing LiDepartment of Biological Chemistry, University of California, Los Angeles, California 90095, USA.
Hiroyuki KagechikaInstitute of Biomaterials and Bioengineering, Tokyo Medical and Dental University, Tokyo 113-8510, Japan.
Peter Tontonoz1] Howard Hughes Medical Institute, Chevy Chase, Maryland 20815, USA [2] Department of Pathology and Laboratory Medicine, University of California, Los Angeles, California 90095, USA.
Vanessa NúñezCardiovascular Development and Repair Department, Centro Nacional de Investigaciones Cardiovasculares (CNIC), Melchor Fernandez Almagro 3, 28029 Madrid, Spain.
Mercedes RicoteCardiovascular Development and Repair Department, Centro Nacional de Investigaciones Cardiovasculares (CNIC), Melchor Fernandez Almagro 3, 28029 Madrid, Spain.
Genhong ChengDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, California 90095, USA.
University of California, Los Angeles · USSpanish National Centre for Cardiovascular Research · ESHoward Hughes Medical Institute · USTokyo Medical and Dental University · JP

Funding

Pilot and Feasibility ProgramP30DK041301 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ROZENGURT, JUAN ENRIQUE · 1990 to 2019
$18.0M
UCLA Tumor Immunology Training ProgramT32CA009120 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Steven M. Dubinett, MICHAEL A TEITELL · 1985 to 2026
$10.3M
Vitamin D Metabolism in LeprosyP50AR063020 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MODLIN, ROBERT L · 2012 to 2016
$7.8M
Viral Mediated Type I Interferon InductionR01AI069120 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHENG, GENHONG · 2006 to 2021
$6.0M
Mechanisms of Biodefense By Toll-Like ReceptorsR01AI056154 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHENG, GENHONG · 2004 to 2014
$3.7M
ROLE OF TOLL-LIKE RECEPTORS IN SKINR37AI047868 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MODLIN, ROBERT L · 2000 to 2009
$2.9M
Divergence of Phagocytic and Antimicrobial Programs in LeprosyR01AI047868 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MODLIN, ROBERT L · 2010 to 2014
$2.4M
Role of IRF3 and RXRa Crosstalk in Host Response to Viral InfectionsR01AI078389 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHENG, GENHONG · 2009 to 2013
$1.8M
Howard Hughes Medical InstituteNCI NIH HHS 5T32CA009120NCI NIH HHS T32 CA009120NIAID NIH HHS AI056154NIAID NIH HHS AI069120NIAID NIH HHS AI47868NIAID NIH HHS NIH RO1 AI078389NIAID NIH HHS R01 AI047868NIAID NIH HHS R01 AI056154NIAID NIH HHS R01 AI069120NIAID NIH HHS R01 AI078389NIAID NIH HHS R37 AI047868NIAMS NIH HHS P50 AR063020NIDDK NIH HHS P30 DK041301
6 · The paper itself

Abstract

The retinoid X receptor α (RXRα), a key nuclear receptor in metabolic processes, is downregulated during host antiviral response. However, the roles of RXRα in host antiviral response are unknown. Here we show that RXRα overexpression or ligand activation increases host susceptibility to viral infections in vitro and in vivo, while Rxra-/- or antagonist treatment reduces infection by the same viruses. Consistent with these functional studies, ligand activation of RXR inhibits the expression of antiviral genes including type I interferon (IFN) and Rxra-/- macrophages produce more IFNβ than WT macrophages in response to polyI:C stimulation. Further results indicate that ligand activation of RXR suppresses the nuclear translocation of β-catenin, a co-activator of IFNβ enhanceosome. Thus, our studies have uncovered a novel RXR-dependent innate immune regulatory pathway, suggesting that the downregulation of RXR expression or RXR antagonist treatment benefits host antiviral response, whereas RXR agonist treatment may increase the risk of viral infections.

Indexed as

Active Transport, Cell NucleusAnimalsbeta CateninCell LineDown-RegulationFatty Acids, UnsaturatedHEK293 CellsHerpes SimplexHerpesvirus 1, HumanHumansInterferon-betaLigandsMacrophagesMaleMiceMice, Inbred C57BLAGN 194204beta CateninFatty Acids, UnsaturatedInterferon-betaLigandsPoly I-CRetinoid X Receptor alphaRNA, Small InterferingTetrahydronaphthalenes

Identifiers

PMID25417649
PMCPMC4380327
OpenAlexW2021438519

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.